|
131
|
|
|
NECAP endocytosis associated 1 |
DEE21, EIEE21 |
Attention deficit hyperactivity disorder, Autism, Brain atrophy, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Spasms x-linked, Status epilepticusView all (4 more) |
|
132
|
|
|
NMDA receptor synaptonuclear signaling and neuronal migration factor |
HH9, NELF |
Anaplastic carcinoma, Anxiety disorder, Carcinoma, Clinodactyly, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular hypogonadismView all (21 more) |
|
133
|
|
|
NOC2 like nucleolar associated transcriptional repressor |
NET15, NET7, NIR, PPP1R112 |
|
|
134
|
|
|
Nephrocystin 4 |
POC10, SLSN4 |
Anemia, Cataract, Ciliopathies, Congenital hepatic fibrosis, Developmental delay, Disorder of eye, Dwarfism, Hypertension, Kidney disease, Nephronophthisis, Premature menopause, Renal corticomedullary cysts, Renal dysplasia and retinal aplasia, Retinal dystrophy, Rod-cone dystrophy, Rotary nystagmus, Senior-loken syndromeView all (2 more) |
|
135
|
|
|
Nuclear protein 1, transcriptional regulator |
COM1, P8 |
|
|
136
|
|
|
Neuronal PAS domain protein 4 |
Le-PAS, NXF, PASD10, bHLHe79 |
|
|
137
|
|
|
Neurobeachin |
BCL8B, LYST2, NEDEGE |
|
|
138
|
|
|
Neuroplastin |
GP55, GP65, SDFR1, SDR1, np55, np65 |
|
|
139
|
|
|
Nephrocystin 3 |
CFAP31, MKS7, NPH3, RHPD, RHPD1, SLSN3 |
Aortic valve sclerosis, Atrial septal defect, Biliary cirrhosis, Cataract, Cholestasis, Ciliopathies, Cirrhosis, Asplenia, Congenital hepatic fibrosis, Pulmonary hypoplasia, Congenital malrotation of intestine, Dandy-walker syndrome, Developmental delay, Disorder of eye, Dwarfism, Fibrosis of pancreas, Hypertension, Kidney disease, Liver cyst, Liver fibrosis, Meckel syndrome, Meckel-like syndrome, Multicystic renal dysplasia, Nephronophthisis, Pancreatic cyst, Patent ductus arteriosus, Polycystic kidney disease, Polydactyly, Polysplenia, Premature menopause, Renal corticomedullary cysts, Renal dysplasia, Renal dysplasia and retinal aplasia, Renal glomerular disease, Renal insufficiency, Renal-hepatic-pancreatic dysplasia, Retinal dystrophy, Senior-loken syndrome, Situs inversusView all (24 more) |
|
140
|
|
|
NADPH oxidase 1 |
GP91-2, MOX1, NOH-1, NOH-1L, NOH1 |
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